Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 12:01 AM
Ignite Modification Date:
2025-12-25 @ 12:01 AM
NCT ID:
NCT05787158
Eligibility Criteria:
Inclusion Criteria:
* Females of 25 to 40 years were included in this study.(20)
* Female patients who gave birth at least 6 months before.(20)
* Females who gave birth through vaginal delivery.(20)
* Females with at least three positive pain provocative tests such as posterior pelvic pain provocation test (P4), active straight leg raise test (ASLR), thigh thrust, Patrick's Faber test, Gaenslen's test and distraction test.(20)
* History of pain around the pelvic girdle, lower back or between the posterior iliac crest and the gluteal fold, difficulty in walking and/or pain when putting weight on one leg
Exclusion Criteria:
* Females who suffered from grade 3 or 4 vaginal tears during their pregnancy (20)
* Females who underwent episiotomy during delivery (20)
* Females who delivered through caesarean section (20)
* Postpartum females with a history of trauma to the pelvic region (20)
* Postpartum females with a history of pelvic surgery
* Postpartum females with a history of other orthopedic disorders
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
25 Years
Maximum Age:
35 Years
Study:
NCT05787158
Study Brief:
Protocol Section:
NCT05787158